A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112025



Internal ID21295291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96382901..96385337hg38UCSC Ensembl
Innerchr9:99145183..99147619hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382437
hg192437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089728
Samplessample149
Known GenesSLC35D2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112025
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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